Sterile Pharmaceutical Manufacturing

The manufacture of sterile products is subject to special requirements in order to minimize the risk of microbiological, particulate and pyrogen contamination. It all depends on the skill, training and attitudes of the personnel involved. Quality Assurance is particularly important, and this type of manufacture must the methods of preparation and procedures strictly followed carefully established and validated. The only remedy for sterility or other quality aspects must not be placed on a terminal process or testing the finished product. The quality and safety of pharmaceutical products is the most important aspect of Sterile Pharmaceutical Manufacturing.

  • Quality control
  • Drugs and Non-drugs
  • Sanitation
  • Manufacture of sterile preparations
  • Sterilization
  • Terminal sterilization
  • Microbial contamination
  • Aseptic processing and sterilization by filtration
  • Isolator technology
  • Blow or fill or seal technology
  • Personnel
  • Premises
  • Equipment
  • Finishing of sterile products
  • Protocols
  • Chemotherapy
  • Microorganisms
  • Applied Microbiology
  • Sterility Testing

Related Conference of Sterile Pharmaceutical Manufacturing

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World Yeast Congress

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Sterile Pharmaceutical Manufacturing Conference Speakers

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